BIODEGRADABLE INJECTABLE IMPLANT SYSTEMS FOR LONG-TERM DRUG-DELIVERY USING POLY(LACTIC-CO-GLYCOLIC) ACID COPOLYMERS

Citation
G. Chandrashekar et N. Udupa, BIODEGRADABLE INJECTABLE IMPLANT SYSTEMS FOR LONG-TERM DRUG-DELIVERY USING POLY(LACTIC-CO-GLYCOLIC) ACID COPOLYMERS, Journal of Pharmacy and Pharmacology, 48(7), 1996, pp. 669-674
Citations number
26
Categorie Soggetti
Pharmacology & Pharmacy
ISSN journal
00223573
Volume
48
Issue
7
Year of publication
1996
Pages
669 - 674
Database
ISI
SICI code
0022-3573(1996)48:7<669:BIISFL>2.0.ZU;2-T
Abstract
Poly (lactide-co-glycolide) (PLG), is one of the most widely employed biodegradable synthetic polymers for sustained-release preparations. I n the present work, PLG (50:50) copolymer has been used to deliver dic lofenac sodium in the form of microspheres and in situ gel-forming sys tems, both of which can be injected subcutaneously. The pharmacodynami c and pharmacokinetic studies in the adjuvant-induced arthritic rats s howed that the microspheres offered steady therapeutic levels of the d rug in the plasma for about 16 days following a single subcutaneous in jection. However, the in situ gel-forming system provided a significan tly higher maximum plasma concentration and increased inhibition of in flammation, maintained for about 10 days. Injectable microspheres and in situ gel-forming implant systems of PLG (50:50) copolymer may there fore be considered as prospective implantable controlled-release dosag e forms to deliver drugs in long-term therapy of chronic ailments.